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Nanoparticles in the clinic

Nanoparticle/microparticle‐based drug delivery systems for systemic (i.e., intravenous) applications have significant advantages over their nonformulated and free drug counterparts. For example, nanoparticle systems are capable of delivering therapeutics and treating areas of the body that other del...

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Detalles Bibliográficos
Autores principales: Anselmo, Aaron C., Mitragotri, Samir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689513/
https://www.ncbi.nlm.nih.gov/pubmed/29313004
http://dx.doi.org/10.1002/btm2.10003
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author Anselmo, Aaron C.
Mitragotri, Samir
author_facet Anselmo, Aaron C.
Mitragotri, Samir
author_sort Anselmo, Aaron C.
collection PubMed
description Nanoparticle/microparticle‐based drug delivery systems for systemic (i.e., intravenous) applications have significant advantages over their nonformulated and free drug counterparts. For example, nanoparticle systems are capable of delivering therapeutics and treating areas of the body that other delivery systems cannot reach. As such, nanoparticle drug delivery and imaging systems are one of the most investigated systems in preclinical and clinical settings. Here, we will highlight the diversity of nanoparticle types, the key advantages these systems have over their free drug counterparts, and discuss their overall potential in influencing clinical care. In particular, we will focus on current clinical trials for nanoparticle formulations that have yet to be clinically approved. Additional emphasis will be on clinically approved nanoparticle systems, both for their currently approved indications and their use in active clinical trials. Finally, we will discuss many of the often overlooked biological, technological, and study design challenges that impact the clinical success of nanoparticle delivery systems.
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spelling pubmed-56895132018-01-08 Nanoparticles in the clinic Anselmo, Aaron C. Mitragotri, Samir Bioeng Transl Med Reviews Nanoparticle/microparticle‐based drug delivery systems for systemic (i.e., intravenous) applications have significant advantages over their nonformulated and free drug counterparts. For example, nanoparticle systems are capable of delivering therapeutics and treating areas of the body that other delivery systems cannot reach. As such, nanoparticle drug delivery and imaging systems are one of the most investigated systems in preclinical and clinical settings. Here, we will highlight the diversity of nanoparticle types, the key advantages these systems have over their free drug counterparts, and discuss their overall potential in influencing clinical care. In particular, we will focus on current clinical trials for nanoparticle formulations that have yet to be clinically approved. Additional emphasis will be on clinically approved nanoparticle systems, both for their currently approved indications and their use in active clinical trials. Finally, we will discuss many of the often overlooked biological, technological, and study design challenges that impact the clinical success of nanoparticle delivery systems. John Wiley and Sons Inc. 2016-06-03 /pmc/articles/PMC5689513/ /pubmed/29313004 http://dx.doi.org/10.1002/btm2.10003 Text en © 2016 The Authors. Bioengineering & Translational Medicine is published by Wiley Periodicals, Inc. on behalf of The American Institute of Chemical Engineers. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Anselmo, Aaron C.
Mitragotri, Samir
Nanoparticles in the clinic
title Nanoparticles in the clinic
title_full Nanoparticles in the clinic
title_fullStr Nanoparticles in the clinic
title_full_unstemmed Nanoparticles in the clinic
title_short Nanoparticles in the clinic
title_sort nanoparticles in the clinic
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689513/
https://www.ncbi.nlm.nih.gov/pubmed/29313004
http://dx.doi.org/10.1002/btm2.10003
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